The Packaging Analyst plays a critical role in ensuring the effectiveness of packaging operations by training and qualifying Inspectors updating SOPs and Work Instructions performing periodic reviews in OneVault creating and maintaining defect qualification sets trending inspection data and supporting investigations and process improvements.
Responsibilities:
- Training/Qualification
- Train and qualify Inspectors for Core 1 Products
- Create and manage defect qualification sets
- Trend batch data from inspection records
- Generate and update controlled documents procedures and work instructions in OneVault
- Initiate document and support change controls (Global Trackwise) and process updates
- Complete and document investigations CAPAs non-conformances root cause analysis and system risk assessments
- Administration/Meetings
- Attend Tier and CAPA Investigation meetings with internal stakeholders
- Support other duties as required
Qualifications :
- Knowledge of regulatory requirements in a pharmaceutical GxP environment
- Minimum 3 years experience in a regulated environment
- Preferred: Experience with S4 HANA OneVault Global Trackwise MS Office
Additional Information :
The deadline for applications for this role is the 20th March 2026
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Work :
No
Employment Type :
Full-time
The Packaging Analyst plays a critical role in ensuring the effectiveness of packaging operations by training and qualifying Inspectors updating SOPs and Work Instructions performing periodic reviews in OneVault creating and maintaining defect qualification sets trending inspection data and supporti...
The Packaging Analyst plays a critical role in ensuring the effectiveness of packaging operations by training and qualifying Inspectors updating SOPs and Work Instructions performing periodic reviews in OneVault creating and maintaining defect qualification sets trending inspection data and supporting investigations and process improvements.
Responsibilities:
- Training/Qualification
- Train and qualify Inspectors for Core 1 Products
- Create and manage defect qualification sets
- Trend batch data from inspection records
- Generate and update controlled documents procedures and work instructions in OneVault
- Initiate document and support change controls (Global Trackwise) and process updates
- Complete and document investigations CAPAs non-conformances root cause analysis and system risk assessments
- Administration/Meetings
- Attend Tier and CAPA Investigation meetings with internal stakeholders
- Support other duties as required
Qualifications :
- Knowledge of regulatory requirements in a pharmaceutical GxP environment
- Minimum 3 years experience in a regulated environment
- Preferred: Experience with S4 HANA OneVault Global Trackwise MS Office
Additional Information :
The deadline for applications for this role is the 20th March 2026
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Work :
No
Employment Type :
Full-time
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